Symbol Name ID |
Rarb
retinoic acid receptor, beta MGI:97857 |
Darker colors indicate more annotations |
Human Phenotypes | Micrognathia |
Retrognathia |
Disease(s) Associated with RARB | ||
syndromic microphthalmia 12 |
Mouse Phenotypes | abnormal basioccipital bone morphology |
absent metoptic pillar |
fusion of atlas and occipital bones |
abnormal skeleton morphology |
fusion of atlas and odontoid process |
split cervical atlas |
split cervical axis |
cervical vertebral transformation |
abnormal vertebral arch morphology |
fusion of vertebral arches |
vertebral transformation |
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Availability | Mouse Genotype | |||||||||||
Rarbtm1Mma/Rarbtm1Mma | ||||||||||||
Rarbtm1Mma/Rarb+ |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 04/16/2024 MGI 6.23 |
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